次黄嘌呤
黄嘌呤
类阿片
化学
药理学
嘌呤
谷胱甘肽
戒毒(替代医学)
氧化应激
代谢组学
抗氧化剂
美沙酮
嘌呤代谢
生物化学
医学
受体
酶
替代医学
病理
色谱法
作者
Paolo Mannelli,Ashwin A. Patkar,Steve Rozen,Wayne R. Matson,Ranga Krishnan,Rima Kaddurah‐Daouk
摘要
Abstract Objective More must be learned about metabolic and biochemical alterations that contribute to the development and expression of drug dependence. Experimental opioid administration influences mechanisms and indices of oxidative stress, such as antioxidant compounds and purine metabolism. We examined perturbations of neurotransmitter‐related pathways in opioid dependence (OD). Methods In this preliminary study, we used a targeted metabolomics platform to explore whether biochemical changes were associated with OD by comparing OD individuals ( n = 14) and non‐drug users ( n = 10). Results OD patients undergoing short‐term methadone detoxification showed altered oxidation–reduction activity, as confirmed by higher plasma levels of α ‐ and γ ‐ tocopherol and increased GSH/GSSG ratio. OD individuals had also altered purine metabolism, showing increased concentration of guanine and xanthosine, with decreased guanosine, hypoxanthine and hypoxanthine/xanthine and xanthine/xanthosine ratios. Other drug use in addition to opioids was associated with partly different biochemical changes. Conclusions This is a preliminary investigation using metabolomics and showing multiple peripheral alterations of metabolic pathways in OD. Further studies should explore the metabolic profile of conditions of opioid abuse, withdrawal and long‐term abstinence in relation to agonist and antagonist treatment and investigate biochemical signatures of opioid substances and medications. Copyright © 2009 John Wiley & Sons, Ltd.
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